Methods and templates for shaping patient-specific anatomical-fixation implants

ABSTRACT

In one embodiment, an anatomical implant template has a template body having opposed first and second terminal ends. The template body bends so as to change the body from a first configuration, whereby the body extends from the first terminal end to the second terminal end along a first path, to a second configuration, whereby the body extends from the first terminal end to the second terminal end along a second path, different from the first path, the second path conforming more closely to the curvature of the at least one anatomical body. The body supports at least one device that outputs at least one signal from which a shape of the body in the second configuration can be ascertained. The anatomical implant template can further communicate the at least one signal to a computing device that generates signals for bending an anatomical implant.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional Application No.62/186,690, filed Jun. 30, 2015, the contents of which are herebyincorporated by reference as if set forth in their entirety herein.

BACKGROUND

Spinal fusion involves joining two or more adjacent vertebrae with ananatomical-fixation implant, and more specifically a spinal-fixationimplant, to restrict movement of the vertebrae with respect to oneanother. For a number of known reasons, spinal-fixation implants areused in spine surgery to align and/or fix a desired relationship betweenadjacent vertebral bodies. Spinal-fixation implants may include, forexample, fixation rods and/or fixation plates having sufficient lengthto span two or more vertebrae and having sufficient rigidity to maintaina fixed relationship between vertebrae under normal physiologicalloading of the spine. Each fixation rod and/or fixation plate may beattached to the vertebrae via various bone-fixation devices such screws,bolts, nails, hooks or the like, that pass through the rods and/orplates into the vertebrae, or may be attached to the vertebrae viavarious bone-fixation devices that are attached to the vertebrae beforereceiving the fixation rods and/or plates, such as bone anchorassemblies having anchor seats with rod-receiving channels.

Typically, the spinal-fixation implant is provided to the surgeon in afirst (e.g., initial or pre-operative) configuration, and must be bentduring surgery to a second (e.g., final or post-operative) configurationthat is curved so as to align the spinal-fixation implant with thedesired, post-operative curvature or contour of the at least oneanatomical body. Before bending the spinal-fixation implant, thepost-operative spinal contour is determined or approximated using arelatively malleable implant template as a guide or pattern. The implanttemplate has a shape or form such as a rod and/or plate that is similarto the form of the spinal-fixation implant, although the curvature ofthe implant template initially might not match that of thespinal-fixation implant. The implant template also has a rigidity thatis less than that of the spinal-fixation implant. Consequently, unlikethe spinal fixation implant, the implant template can be bent by hand.However, due to the ease with which the implant template can be bent,the implant template itself is not suitable for use as a spinal-fixationimplant as the implant template would not maintain a fixed relationshipbetween vertebrae under normal physiological loading of the spine.

In operation, the implant template is positioned into the target area ofthe spine, and the implant template is bent by hand from an initialcontour to the desired final or post-operative contour. Upon achievingthe final spinal contour, the implant template is removed from thespine, and the spinal-fixation implant is bent using a manualhand-operated bending tool so as to match the post-operative contour ofthe implant template. As the spinal-fixation element is bent, thesurgeon holds the spinal-fixation implant and the implant templateadjacent to one another so as to compare the contour of thespinal-fixation implant with the final contour of the implant template.The surgeon continues this process of bending the spinal-fixationimplant and comparing it with the implant template until the finalcontour is achieved. The bending can be performed in multiple steps soas to obtain one or more intermediate contours between the initialcontour and the final contour. Once the final contour is achieved, thespinal-fixation implant is implanted into the spine by attaching thespinal-fixation implant to the vertebrae.

BRIEF DESCRIPTION OF THE DRAWINGS

The foregoing summary, as well as the following detailed description ofembodiments of the application, will be better understood when read inconjunction with the appended drawings. For the purposes of illustratingthe methods and devices of the present application, there is shown inthe drawings representative embodiments. It should be understood,however, that the application is not limited to the precise methods anddevices shown. In the drawings:

FIG. 1 shows a simplified schematic diagram of a system according to oneembodiment configured to bend an anatomical-fixation implant to conformto a curvature of at least one anatomical body;

FIG. 2 shows a perspective side view of an anatomical implant templateaccording to one embodiment in a first configuration;

FIG. 3 shows a perspective side view of the anatomical implant templateof FIG. 2 in a second configuration;

FIG. 4 shows a cross-sectional view of the anatomical implant templateof FIGS. 2 and 3 according to one embodiment;

FIG. 5 shows a cross-sectional view of the anatomical implant templateof FIGS. 2 and 3 according to another embodiment;

FIG. 6 shows an exploded perspective end view of the anatomical implanttemplate of FIGS. 2 and 3 according to another embodiment;

FIG. 7 shows an exploded perspective end view of the anatomical implanttemplate of FIGS. 2 and 3 according to another embodiment;

FIG. 8 shows an exploded perspective end view of the anatomical implanttemplate of FIGS. 2 and 3 according to another embodiment;

FIG. 9 shows a top perspective view of an anatomical implant templateaccording to another embodiment in a first configuration;

FIG. 10 shows a top perspective view of the anatomical implant templateof FIG. 9 in a second configuration;

FIG. 11 shows a cross-sectional view of the anatomical implant templateof FIGS. 9 and 10 according to one embodiment;

FIG. 12 shows a top view of the anatomical implant template of FIGS. 9and 10 according to another embodiment;

FIG. 13 shows a perspective view of the anatomical implant template ofFIGS. 9 and 10 according to yet another embodiment;

FIG. 14 shows a perspective view of the at least one sensor of FIG. 13according to one embodiment;

FIG. 15 shows a perspective view of the at least one sensor of FIG. 13according to another embodiment;

FIG. 16 shows a simplified flow diagram of a method of operating theanatomical implant template of FIG. 1 according to one embodiment; and

FIG. 17 shows a simplified flow diagram of a method of manipulating theanatomical-fixation implant of FIG. 1 according to one embodiment.

DETAILED DESCRIPTION

Certain terminology is used in the following description for convenienceonly and is not limiting. The words “right”, “left”, “lower” and “upper”designate directions in the drawings to which reference is made. Thewords “inner” and “outer” refer to directions toward and away from,respectively, the geometric center of the bone screw and related partsthereof. The terminology includes the above-listed words, derivativesthereof and words of similar import.

The technique of manually bending the spinal-fixation implant bycomparing the spinal-fixation implant to an implant template asdescribed above in the background section can have several drawbacks.For instance, bending the spinal-fixation implant in such a manner canresult in operator error in trying to match the spinal-fixation implantto the implant template such that the bent spinal-fixation implantincludes bends that do not adequately match the bends of the implanttemplate. Attempting to remove or correct these incorrectly-formed bendscan result in over bending of the spinal-fixation implant, which canweaken the spinal-fixation implant. Moreover, incorrectly-formed bendscan be difficult, if not impossible, to remove completely.

Therefore, there is a need for improved tools and methods for bendingspinal-fixation implants, and similarly for bending anatomical-fixationimplants other than those used in the spine, such as orthopedicimplants, cranio-maxillo-facial implants, dental implants, and otherimplants that are intra-operatively shaped to fit the anatomy. Althoughthe following example embodiments pertain specifically tospinal-fixation implants, it will be understood that, unless explicitlystated otherwise, the tools and methods described herein may be used forbending anatomical-fixation implants other than spinal-fixationimplants, including implants used in locations other than in the spine.

Referring to the schematic of FIG. 1, a system 100 is shown that isconfigured to bend an anatomical-fixation implant 110 so as to conformthe anatomical-fixation implant 110 to a curvature of at least oneanatomical body, and preferably, to a desired post-operative curvatureof the at least one anatomical body. The anatomical-fixation implant 110can include a body defining (without limitation) a rod, a plate, a shapehaving at least one rod-shaped portion and at least one plate-shapedportion, or any other shape suitable for fixing a position of one ormore anatomical bodies. Further, the anatomical-fixation implant 110 hasa length sufficient to extend at least from a first vertebra to a secondvertebra. The at least one anatomical body can include any anatomicalbody having a curvature, including (without limitation) one or more of along bone, a vertebra, at least a portion of a spinal column, and bonesspanning a joint such as the wrist or ankle. The at least a portion of aspinal column can include a plurality of vertebrae up to an entirety ofa spinal column, and can also include one or both of a skull and asacrum. The curvature of the at least one anatomical body can be definedby at least one exterior surface of the at least one anatomical body.Alternatively or additionally, the curvature of the at least oneanatomical body can be defined by at least one of an interior surface ofthe at least one anatomical body such as an intramedullary canal.

System 100 includes an anatomical implant template 102 and a computingdevice 104 that is in wired and/or wireless communication with theanatomical implant template 102. The anatomical implant template 102 isused as a guide or pattern to bend the anatomical-fixation implant 110so as to conform the anatomical-fixation implant 110 to the curvature ofthe anatomical implant template 102. In general, the anatomical implanttemplate 102 can be selected to have a form that corresponds to the formof the anatomical-fixation implant 110. For example, if theanatomical-fixation implant 110 defines a rod such as a spinal rod, thenthe anatomical implant template 102 can also define a rod. In such acase, the anatomical implant template 102 can be chosen such that thewidth, thickness, and/or diameter of the anatomical implant template 102is equal to, or substantially equal to, that of the anatomical-fixationimplant 110. The anatomical implant template 102 can also be selected tohave a length that is less than, equal to, or greater than the length ofthe anatomical-fixation implant 110. Similarly, when theanatomical-fixation implant 110 defines a plate, the anatomical implanttemplate 102 can also define a plate. In such a case, the anatomicalimplant template 102 can have a length, width, and/or thickness that isequal to, or substantially equal to, that of the anatomical-fixationimplant 110.

As will be described in further detail below, the anatomical implanttemplate 102 has a flexible template body that can be bent by hand to acurvature of the at least one anatomical body, and preferably, to adesired post-operative curvature of the at least one anatomical body.The template body supports at least one device that outputs a signal 114from which the curvature of the anatomical implant template 102 can beascertained. For example, the device can be at least one sensor thatoutputs at least one sensor signal from which the curvature of theanatomical implant template 102 can be ascertained. Alternatively, theat least device can be a radio-frequency identification (RFID) devicethat outputs the signal 114 to an RFID receiver. The at least one signal114 can be indicative of absolute position of points along theanatomical implant template 102, or can be indicative of positionalchange of the anatomical implant template 102 from a first configurationto a second configuration. Further, the anatomical implant template 102is configured to communicate the at least one signal 114 to thecomputing device 104 via a wireless, wired, or optical connection. Thus,the at least one signal can be, for example, an electrical signal or anoptical signal.

The computing device 104 is configured to receive the at least onesignal 114 from the anatomical implant template 102 and generate implantbending signals 116. The computing device 104 can also generate acomputer model of the shape and curvature of the anatomical implanttemplate 102, which can in turn be used to generate the implant bendingsignals 116. The system 100 can further include a computer-controlledbending machine 106 that is in wired and/or wireless communication withthe computing device 104. The computing device 104 can be physicallyintegrated with the computer-controlled bending machine 106.Alternatively, the computing device can be physically separate andspaced from the computer-controlled bending machine 106, and cancommunicate the implant bending signals 116 to the computer-controlledbending machine 106 via a wired or wireless connection. Note that,according to various embodiments, a system can include one or more ofthe computing device 104, the computer-controlled bending machine 106,and the anatomical implant template 102. For example, a system can beenvisioned that includes the computing device 104 and thecomputer-controlled bending machine 106, without the anatomical implanttemplate 102.

The computer-controlled bending machine 106 is configured to receive theanatomical-fixation implant 110 in a first or pre-operative implantconfiguration 108. In at least some embodiments, the anatomical-fixationimplant 110 in the pre-operative implant configuration 108 can be apiece of stock material. For example, the anatomical-fixation implant110 can be a rod, a plate, or a body having at least one rod-shapedportion and at least one plate-shaped portion. Further, theanatomical-fixation implant 110 can be a relatively stiff material thatis not bendable by hand so as to be capable of resisting bending whenimplanted into the body and subjected to anatomical loading. In otherwords, the anatomical-fixation implant 110 can have sufficient strengthto resist bending when subjected to anatomical loading. Thecomputer-controlled bending machine 106 is configured to bend theanatomical-fixation implant 110 into a second or post-operative implantconfiguration 112 based on the implant bending signals, where thepost-operative implant configuration 112 conforms more closely to theshape and curvature of the anatomical implant template 102, and hencemore closely to the curvature of the at least one anatomical body.Bending is performed automatically by the computer-controlled bendingmachine 106, as opposed to manually by hand. However, in alternativeembodiments, the system 100 can include a hand-operated bending device(not shown), in lieu of or in addition to the computer-controlledbending machine 106, and an operator such as a surgeon can bend theanatomical-fixation implant 110 during a surgical procedure using thehand-operated bending device. In such alternative embodiments, thecomputing device 104 can include a display screen or audio deviceconfigured to communicate instructions for bending theanatomical-fixation implant 110 to the user.

Referring to FIGS. 2 and 3, an anatomical implant template 200 is shownin first and second configurations, respectively, the firstconfiguration having a first curvature and the second configurationhaving a second curvature, different from the first curvature. Theanatomical implant template 200, which can be used to implement thetemplate 102 of FIG. 1, includes a template body 202 that defines a rodand further includes at least one sensor (discussed further below inrelation to FIGS. 4 to 8) coupled, either directly or indirectly, to thetemplate body 202. The anatomical implant template 200 has a firstterminal end surface 204, a second terminal end surface 206 spaced fromthe first terminal end surface 204, and an outer surface 207 thatextends from the first terminal end surface 204 to the second terminalend surface 206. The first and second terminal end surfaces 204 and 206are spaced from one another by a dimension D_(K) that is measured alonga straight line SL from the first terminal end surface 204 to the secondterminal end surface 206. The dimension D_(SL) is dependent on thecurvature of the anatomical implant template 200, and therefore, thedimension D_(SL) can vary as the curvature of the anatomical implanttemplate 200 is changed.

The anatomical implant template 200 extends from the first terminal endsurface 204 to the second terminal end surface 206 along a center lineCL that extends through a substantial geometric center of the anatomicalimplant template 200. The anatomical implant template 200 has anouter-most or overall dimension or length L1 that is measured along thecenter line CL from the first terminal end surface 204 to the secondterminal end surface 206. The anatomical implant template 200 also has aplurality of cross-sections along the length L1 of the anatomicalimplant template 200, each cross-section extending in a plane that isperpendicular to the center line CL. Each cross-section can have anysuitable cross-sectional size and shape, such as (without limitation) acircle as shown, an oval, a square, or a rectangle, and the size andshape of the cross-sections may be constant along the length L1 as shownor may vary.

Each cross-section has a first outer-most or overall cross-sectionaldimension D1 along a first direction that is perpendicular to the centerline CL, and a second outer-most or overall cross-sectional dimension D2along a second direction that is perpendicular to the first directionand to the center line CL. In the embodiment of FIGS. 2 and 3, eachcross-section of the anatomical implant template 200 has a substantiallycircular shape, wherein the first cross-sectional dimension D1 and thesecond cross-sectional dimension D2 are an outer-most or overalldiameter of the anatomical implant template 200. In other embodiments,such as anatomical implant templates that have square, rectangular,oval, or other shape, each cross-section can have a cross-sectionaldimension D1 such as a width that is less than, greater than, or equalto, a second cross-sectional dimension D2 such as a thickness.

The anatomical implant template 200 is elongate along the center lineCL. Thus, the length L1 is greater than both the first and secondcross-sectional dimensions D1 and D2. The length L1 is independent ofthe curvature of the anatomical implant template 200, and therefore, thelength L1 remains constant as the curvature of the anatomical implanttemplate 200 is changed. Further, the length L1 can have any suitablevalue. For example, in embodiments wherein the anatomical implanttemplate 200 is used in a spine, the anatomical implant template 200 canhave a length L1 that extends across at least two anatomical bodies suchas across at least two vertebrae or across at least one vertebrae andthe skull or sacrum. The first and second cross-sectional dimensions D1and D2 can be a size suitable for attaching to the at least oneanatomical body. For example, the anatomical implant template 200 candefine first and second cross-sectional dimensions D1 and D2 that aresuitable for installation into a rod-receiving recess of each of one ormore bone anchor assemblies where the bone anchor assemblies are used toaffix the anatomical-fixation implant to a spine.

The anatomical implant template 200 is configured to bend along thecenter line CL at one or more bending locations between the firstterminal end surface 204 and the second terminal end surface 206. In atleast some embodiments, the anatomical implant template 200 bends alongat least a portion, up to an entirety, of the length L1 of theanatomical implant template 200 between the first and second terminalend surfaces 204 and 206. For example, the anatomical implant template200 can include a bending location that extends continuously along thecenter line CL along the at least a portion, up to an entirety, of thelength L1 of the anatomical implant template 200. Alternatively, theanatomical implant template 200 can include a plurality of bendinglocations, each of which extends continuously along the center line CLalong a different portion of the anatomical implant template 200.Alternatively still, the bending locations can be defined by discretebending points along the center line CL along at least a portion, up toan entirety, of the length L1 of the anatomical implant template 200,where the discrete bending points are spaced from one another along thecenter line CL. For illustrative purposes, FIG. 3 shows the anatomicalimplant template 200 having two bends that combine to form an s-shape;however, the user can bend the anatomical implant template 200 can haveas few as one bend or more than two bends.

The anatomical implant template 200 is configured to bend at the bendinglocations so as to change the anatomical implant template 200 from afirst configuration, whereby the anatomical implant template 200 extendsfrom the first terminal end surface 204 to the second terminal endsurface 206 along a first path P1, to a second configuration, wherebythe anatomical implant template 200 extends from the first terminal endsurface 204 to the second terminal end surface 206 along a second pathP2, different from the first path P1. The first and second paths P1 andP2 can be co-linear with, or extend parallel to, the center line CL. Thefirst path P1 has a first curvature, and the second path P2 has a secondcurvature, different from the first curvature. In at least someembodiments, the first configuration is an initial or pre-operativeconfiguration, and the second configuration is a subsequent orpost-operative configuration, where the subsequent or post-operativeconfiguration can conform more closely to the desired, post-operativecurvature or contour of the at least one anatomical body than theinitial or pre-operative configuration.

It will be understood that the first and second paths P1 and P2 shown inFIGS. 2 and 3 are merely examples and that, in practice, the first andsecond paths P1 and P2, and hence the first and second curvatures, canvary from that shown in FIGS. 2 and 3. The first path P1 can define acurvature such as a lordotic curvature or other curvature, or can extendalong a straight line. The second path can define an s-shaped curvatureas shown, a lordotic curvature, a parabolic curvature, or any otherdesired, post-operative curvature of the at least one anatomical body.In at least some embodiments, the anatomical implant template 200 isfurther configured to bend at the bending locations so as to change thetemplate body 202 from the second configuration back to the firstconfiguration or to a third configuration having a curvature differentfrom both the first and second configurations.

The anatomical implant template 200 is configured to bend at each of thebending locations along the center line CL towards any direction that isperpendicular to the center line CL at the bending location. Forexample, the anatomical implant template 200 can bend at each bendinglocation about a respective axis A of rotation, where each respectiveaxis A of rotation extends through its respective bending location alonga direction that is perpendicular to the center line CL at therespective bending location. Further, the template body 202 defines aradius of curvature R at each bending location.

In the configuration of FIG. 2 (i.e., the first configuration), theanatomical implant template 200 is shown with a single bend or curvethat has a peak at point 208 a. The anatomical implant template 200 isbent or curved about an axis A₁ of rotation that extends through thepoint 208 a. Further, the anatomical implant template 200 has a firstradius R₁ of curvature at the point 208 a. In the configuration of FIG.3 (i.e., the second configuration), the anatomical implant template 200is shown with two bends or curves that have respective peaks at points208 b and 208 c. The anatomical implant template 200 is bent or curvedabout respective axes A₂ and A₃ of rotation that extend through thepoints 208 b and 208 c, respectively. Further, the anatomical implanttemplate 200 has second and third radii R₂ and R₃ of curvature at thepoints 208 b and 208 c, respectively.

In FIGS. 2 and 3, the anatomical implant template is changed from afirst configuration having a single curve with a first peak 208 a to asecond configuration having two curves with first and second peaks 208 band 208 c. The locations of the peaks 208 b and 208 c along the centerline CL are different from the locations of the peak 208 a. Further, theradii R₂ and R₃ of curvature at the peaks 208 b and 208 c is differentfrom the radius R₁ of curvature of the peak 208 a. However, it will beunderstood that the first and second configurations may vary from thoseshown. In particular, the anatomical implant template 200 can be changedfrom a first configuration having zero or more curves to a secondconfiguration having at least one curve. Further, the locations of thepeaks the curves along the center line CL can vary from the locationsshown in FIGS. 2 and 3.

The center line CL can lie in a single plane in one or both of the firstand second configurations. For example, in spine applications, theanatomical implant template 200 can be bent such that, when theanatomical implant template 200 is positioned along the spine, thecenter line CL lies in a single plane in the spine, where the singleplane is the sagittal plane or the coronal plane. Alternatively, theanatomical implant template 200 can be bent such that the center line CLcan lie in multiple planes in one or both of the first and secondconfigurations. For example, in spine applications, the multiple planescan include one or more of the sagittal plane and the coronal plane.

Turning now to FIGS. 4 to 8, various embodiments of the anatomicalimplant template 200 of FIGS. 2 and 3 are shown. In each embodiment, theanatomical implant template 200 includes a template body 202 and atleast one sensor 220 coupled to the template body 202. The template body202 is configured to bend so as to change the anatomical implanttemplate 200 from the first configuration to the second configuration.The at least one sensor 220 is configured to output at least one sensorsignal from which the curvature of the anatomical implant template 200in the second configuration can be ascertained. In at least someembodiments, the at least one sensor 220 can additionally generate theat least one sensor signal. Further, in at least some embodiments, theat least one sensor 220 can modify an input signal so as to produce amodified signal from which the curvature of the anatomical implanttemplate 200 in the second configuration can be ascertained.

The template body 202 includes a flexible body 210 that extends along,or substantially parallel to, the center line CL between the firstterminal end surface 204 and the second terminal end surface 206. Thetemplate body 202 can extend from the first terminal end surface 204toward the second terminal end surface 206, and terminate at or beforethe second terminal end surface 206. Similarly, the template body 202can extend from the second terminal end surface 206 toward the firstterminal end surface 204, and terminate at or before the first terminalend surface 204. Alternatively, the template body 202 can extend along aportion or portions of the anatomical implant template 200 between thefirst and second terminal end surfaces 204 and 206, and terminate beforeone or both of the first and second terminal end surfaces 204 and 206.In other words, the template body 202 can have a first terminal end anda second terminal end. The first terminal end of the template body 202can be coincident with the first terminal end surface 204 of the implanttemplate 200 or can be located between the first and second terminal endsurfaces 204 and 206. Similarly, the second terminal end of the templatebody 202 can be coincident with the second terminal end surface 204 orcan be located between the first and second terminal end surfaces 204and 206.

The flexible body 210 can include any suitable malleable material orcombination of malleable materials that permits the template body 202 tobe conformed to the desired post-operative contour of the at least oneanatomical body. The malleable material or combination of materials mayinclude one or more of a metal such as annealed aluminum, a metal alloysuch as Nitinol, and a polymer. The flexible body 210 can include aplastically-deformable material configured to maintain the template body202 in the second configuration. Alternatively, or in addition, theflexible body 210 can include an elastically-deformable materialconfigured to return the template body 202 to the first configurationfrom the second configuration.

With continuing reference to FIGS. 2 to 8, the anatomical implanttemplate 200 supports at least one sensor 220 along or substantiallyparallel to the center line CL between the first and second terminal endsurfaces 204 and 206. The at least one sensor 220 is configured outputat least one sensor signal from which the shape of the anatomicalimplant template 200 in the second configuration can be ascertained. Theat least one sensor 220 can include a sensor body 222 having a firstterminal sensor end, a second terminal sensor end spaced from the firstterminal sensor end, and a first surface 222 a, such as an externalsurface, that extends between the first and second terminal sensor ends.The sensor body 222 can be elongate from the first terminal sensor endto the second terminal sensor end.

The sensor body 222 can extend from the first terminal end surface 204of the implant template 200 toward the second terminal end surface 206of the implant template 200, and terminate at or before the secondterminal end surface 206. Similarly, the sensor body 222 can extend fromthe second terminal end surface 206 toward the first terminal endsurface 204, and terminate at or before the first terminal end surface204. Alternatively, the sensor body 222 can extend along a portion orportions of the template body 202 between the first and second terminalend surfaces 204 and 206, and terminate before one or both of the firstand second terminal end surfaces 204 and 206. In other words, the firstterminal sensor end can be coincident with the first terminal endsurface 204, or can be located between the first and second terminal endsurfaces 204 and 206. Similarly, the second sensor end can be coincidentwith the second terminal end surface 204 or can be located between thefirst and second terminal end surfaces 204 and 206. The sensor body 222can be coupled to the template body 202 such that at least a portion ofthe sensor body 222 is aligned with at least one of the bendinglocations along a direction that is perpendicular to the center line CL,such as along a radial direction. Accordingly, when the template body202 is bent at the at least one bending location, the sensor body 222 isalso bent at the at least one bending location.

Alternatively or in addition, the at least one sensor 220 can include aplurality of discrete sensor bodies 222 spaced from one another betweenthe first and second terminal end surfaces 204 and 206. When discretesensor bodies 222 are employed, changes in the shape of the templatebody 202 between the discrete sensors can be determined throughextrapolation. In either case, the elongate sensor body 222 and/or theplurality of discrete sensor bodies 222 can be coupled to the templatebody 202 so as to be aligned with at least one of the bending locationssuch that the at least one sensor 220 bends at the at least one bendinglocation. Alternatively, the sensor body 222 and/or the plurality ofdiscrete sensor bodies 222 can be coupled to the template body 202 so asto be positioned between (i) at least one of the bending locations and(ii) another of the bending locations, the first terminal end surface204, or the second terminal end surface 206 such that a position of theat least one sensor 220 changes relative to the at least one of thebending locations as the template body 202 is bent about the at leastone of the bending locations.

The at least one sensor 220 can include any suitable sensor orcombination of sensors that can sense the shape of the template body 202in the second configuration. The at least one sensor 220 can be anactive sensor that actively transmits a signal or a passive sensor. Theat least one sensor 220 can include, for example, one or more positionsensors that measure absolute position of the template body 202 in thesecond configuration or relative position such as displacement of thetemplate body 202 from the first configuration to the secondconfiguration. In at least some embodiments, the at least one sensor 220can include one or more piezoelectric sensors. The piezoelectric sensorscan be used to measure changes in or more of pressure, strain, andforce, and convert these measured changes into an electrical charge thatcan form the at least one sensor signal.

In at least some embodiments, the at least one sensor 220 can include anoptical sensor such as those used in fiber optic shape sensing. Forexample, the at least one sensor 220 can include an optical fiber havingone or more Fiber Bragg Grating (FBG) sensors. Each FBG sensor is aseries of optical filters that reflect a different wavelength orwavelengths while letting other wavelengths pass through. The FBGsensors respond to strain resulting from stress or pressure on theanatomical implant template. As the optical fiber is bent, therefractive index of the FBG sensors varies, thereby dictating whichwavelengths pass through and which are reflected. These variations canthen be converted to displacement data that can be used to determine theshape of the anatomical implant template.

Turning now to FIG. 4, an embodiment is shown in which the template body202 includes a flexible body 210 and can optionally include a protectivecovering 214. The flexible body 210 defines a tube having a firstsurface 210 a, such as an external surface, and a second surface 210 b,such as an internal surface. The internal surface 210 b is spaced closerto the center line CL than the external surface 210 a. Moreover, theexternal and internal surfaces 210 a and 210 b extend between the firstand second terminal ends of the template body 202. The internal surface210 b defines a channel 212 that extends through an entirety or aportion of the length of the flexible body 210, and supports the atleast one sensor 220. The at least one sensor 220 defines a rod having acircular cross-section, although the rod can define cross-sectionshaving another suitable shape such as a square, rectangle, or oval.

The implant template 200 has a plurality of cross-sections along thecenter line CL, where each cross-section is in a plane that isperpendicular to the center line CL. In each cross-section, the externaland internal surfaces 210 a and 210 b of the flexible body 210 candefine any suitable cross-sectional shape, such as (without limitation)a circle as shown, an oval, a square, or a rectangle. Moreover, theinternal surface 210 b of the flexible body 210 can define a closedshape around the channel 212. In each cross-section, the internalsurface 210 b can define an overall dimension D3 in a planeperpendicular the center line CL, such as a diameter or width of thechannel 212, where the overall dimension D3 is greater than or equal toan outer-most or overall dimension D4 of the at least one sensor 220measured in the same plane. Thus, the channel 212 is sized andconfigured to receive the at least one sensor 220 therein such that thechannel 212 supports the at least one sensor 220 between the first andsecond terminal end surfaces 204 and 206.

FIG. 6 shows an alternative embodiment where the flexible body 210defines a channel 212 that extends into the external surface 210 a ofthe flexible body 210, such that the channel 212 is open along theexternal surface 210 a. Thus, the flexible body 210 can define anopening 216 that is open to the channel 212, where the opening 216 hasan overall dimension or width D6 along a plane that is perpendicular tothe center line CL. For instance, the flexible body 210 can include apair of opposed edges 210 c that define the opening 216 therebetween.The opposed edges 210 c are spaced from one another by the overalldimension D6 in a plane perpendicular to the center line CL. The overalldimension D6 can be less than, greater than, or equal to the overalldimension D4 of the at least one sensor 220. Note that the channel 212can be radially offset from the center line CL as shown, or can beco-linear with the center line CL.

In embodiments where the overall dimension D6 of the opening 216 is lessthan the overall dimension D4 of the at least one sensor 220, the atleast one sensor 220 can snap into the channel 212. For example, the atleast one sensor 220 can compress to a dimension less than the overalldimension D4 as the at least one sensor 220 is passed through theopening 216, and then the at least one sensor 220 expand substantiallyback to the overall dimension D4 once the at least one sensor 220 isreceived in the channel 212. Alternatively, the pair of opposed edges210 c can spread apart by a distance greater than the overall dimensionD6 as the at least one sensor 220 is received through the opening 216,and then the opening 216 can return substantially to the overalldimension D6 once the at least one sensor 220 is received in the channel212. Once the at least one sensor 220 is disposed in the channel 212,the opposed edges 210 c can retain the at least one sensor 220 in thechannel 212.

Referring back to FIG. 4, the template body 202 can also include aprotective covering 214 that covers at least a portion, up to anentirety, of the external surface 210 a of the flexible body 210. Theprotective covering 214, if employed, can define a closed shape aroundthe flexible body 210 in a plane perpendicular to the center line CL.The protective covering 214 can be a coating that is formed over theexternal surface 210 a of the flexible body 210, or can be a separatesheath that is wrapped or translated over the first surface 210 a of theflexible body 210.

Referring to FIG. 5, an embodiment is shown in which the template body202 includes the flexible body 210 and a protective covering 214. Theflexible body 210 defines a rod or a bar having an external surface 210a that extends between the first and second terminal ends of thetemplate body 202. The rod or bar can have a flattened cross-section asshown or another suitable cross-sectional shape. The protective covering214 covers at least a portion of the flexible body 210 between the firstand second terminal ends of the template body 202, and has an internalsurface 214 a that defines a channel 224 that extends at least partiallythrough the protective covering 214. The internal surface 214 a of theprotective covering 214 defines an overall dimension D5, such as adiameter or width, in a plane perpendicular to the center line CL, wherethe overall dimension D5 is greater than a combined dimension of theflexible body 210 and the at least one sensor 220 in the same plane.Thus, the channel 224 is sized to receive both the flexible body 210 andthe at least one sensor 220 such that the at least one sensor 220 iscoupled to the flexible body between the flexible body 210 and at leasta portion of the protective covering 214.

Turning now to FIG. 7, an embodiment of an anatomical implant template200 is shown having a flexible body 210 that can be a conventionaltemplate, and the at least one sensor 220 can be permanently coupled to,or removeably coupled to (e.g., snapped on), the flexible body 210 so asto convert the conventional template into a smart template that isconfigured to output at least one sensor signal from which the shape ofthe anatomical implant template 200 can be ascertained. In embodimentswhere the at least one sensor 210 is removeably coupled to the flexiblebody 210, the flexible body 210 can be reused after cleaning as withconventional templates. Further, the at least one sensor 210 can bedisposable or can be configured to survive cleaning such that the atleast one sensor 210 can be reused.

The flexible body 210 defines a rod or a bar having an external surface210 a that extends between the first and second terminal ends of thetemplate body 202. The flexible body 210 defines a cross-sectionalshape, such as (without limitation) a circle as shown, an oval, asquare, or a rectangle. Moreover, in each cross-section, the flexiblebody 210 can have an outer-most dimension or width D7.

The at least one sensor 220 defines a tube having a first surface 220 a,such as an external surface, and a second surface 220 b, such as aninternal surface. The internal surface 220 b is spaced closer to thecenter line CL than the external surface 220 a. The internal surface 220b defines a channel 226 that extends through an entirety or a portion ofthe length of the at least one sensor 220. Moreover, the external andinternal surfaces 220 a and 220 b extend between the first and secondterminal sensor ends.

The at least one sensor 220 has a plurality of cross-sections along thecenter line CL, where each cross-section is in a plane that isperpendicular to the center line CL. In each cross-section, the externaland internal surfaces 220 a and 220 b of the at least one sensor 220 candefine any suitable cross-sectional shape, such as (without limitation)a circle, an oval, a square, or a rectangle. In each cross-section, theinternal surface 220 b can define an overall dimension D8 in a planeperpendicular the center line CL, such as a diameter or width of thechannel 226, where the overall dimension D8 is greater than or equal toan overall dimension D7 of the flexible body 210 measured in the sameplane. Thus, the channel 226 can be sized and configured to receive theflexible body 210 therein such that the flexible body 210 supports theat least one sensor 220 between the first and second terminal endsurfaces 204 and 206.

Moreover, the internal surface 220 b of the at least one sensor 220 candefine a closed shape around the channel 226, such that the flexiblebody 210 is slidably received in the channel 26. Alternatively, the atleast one sensor 220 can define an open shape or a shape that isconfigured to open so that the at least one as sensor 220 can be wrappedaround the flexible body 210 as the flexible body 210 is received intothe channel 226 along a direction that is perpendicular to the centerline CL. More specifically, the at least one sensor 220 can defineopposed edges 220 c. The opposed edges 220 c can be spaced from oneanother so as to define an opening 228 that is open to the channel 226,where the opening 228 has an overall dimension or width D9 along a planethat is perpendicular to the center line CL. Alternatively, the opposededges 220 c can overlap one another such that the overlapping edges 220c can be separated so as to receive the flexible body 210 into thechannel 226, and then can return to their overlapping state so as toretain the flexible body 210 therein.

Turning now to FIG. 8, an embodiment is shown in which the flexible body210 defines a rod or a bar having an external surface 210 a that extendsbetween the first and second terminal ends of the template body 202. Theflexible body 210 defines a cross-sectional shape, such as (withoutlimitation) a circle as shown, an oval, a square, or a rectangle. The atleast one sensor 220 can be an elongate sensor that is capable of beingtensioned. In this embodiment, a single sensor 220 is shown; however,the implant template may include more than one sensor 220 spaced aroundthe external surface 210 a of the flexible body 210.

To tension the at least one sensor 220 along the flexible body 210, theimplant template 200 can include at least one end cap 230, such as apair of end caps. Each end cap 230 defines a recess 232 that is sizedand shaped to receive a terminal end 234 of the flexible body 210 suchthat the end caps 230 are spaced from one another along the center lineCL. Moreover, at least one of the end caps 230 can comprise a tensioningdevice such as a spring loaded tensioner 236 that applies tension to theat least one sensor 220.

Returning to FIGS. 2 and 3, the anatomical implant template 200 isconfigured to communicate the at least one sensor signal to a computingdevice such as the computing device 104 of FIG. 1 via a wired orwireless connection. The at least one sensor 220 can be configured tocommunicate the at least one sensor signal directly to the computingdevice. Alternatively, the anatomical implant template 200 can includeat least one transmitter 218 coupled to the template body 202 andconfigured to communicate the at least one sensor signal. The at leastone transmitter 218 can be coupled to the template body 202 at one ofthe first and second terminal end surfaces 204 and 206 or can besupported anywhere between the first and second terminal end surfaces204 and 206. The at least one transmitter 218 can include a wirelesstransmitter configured to wirelessly communicate the at least one sensorsignal to the computing device.

Further, the at least one transmitter 218 can include a power supplythat is coupled to the template body 202, where the power supply isconfigured to power the at least one transmitter 218. Alternatively, theat least one transmitter 218 can be powered by a power supply that isnot coupled to the template body 202, such as a power supply that iscoupled to a receiver such as a radio-frequency identification (RFID)receiver, where the receiver that transmits radio energy to a devicecoupled to the template body 202, and the device uses the radio energyto output a response to the receiver. In the case of a wired connection,the anatomical implant template 200 can be coupled to a cable thatcarries the at least one sensor signal from the anatomical implanttemplate 200 to the computing device.

Referring now to FIGS. 9 and 10, an anatomical implant template 300according to another embodiment is shown in first and secondconfigurations, respectively. The anatomical implant template 300, whichcan be used to implement the template 102 of FIG. 1, defines a platethat is configured to conform to a curvature of at least one anatomicalbody. The anatomical implant template 300 comprises a template body 302and at least one sensor 324 (shown in FIGS. 11-15) coupled, eitherdirectly or indirectly, to the template body 302. The anatomical implanttemplate 300 can also define one or more apertures 328 that extendentirely through the template body 302, each of the apertures 328configured to receive, for example, a bone screw or pin therethrough tofix the anatomical implant template 300 to the at least one anatomicalbody.

The anatomical implant template 300 has a first terminal end surface 304and an opposed second terminal end surface 306 spaced from the firstterminal end surface 304. The anatomical implant 300 further has firstand second opposed side surfaces 308 and 310 that extend from the firstterminal end surface 304 to the second terminal end surface 306. Theanatomical implant 300 yet further has opposed upper and lower surfaces312 and 314 that extend from the first terminal end surface 304 to thesecond terminal end surface 306 and from the first side surface 308 tothe second side surface 310. The lower surface 314 can be considered abone-facing surface that is configured to face the at least oneanatomical body when the anatomical implant template 300 is attached tothe at least one anatomical body.

The anatomical implant template 300 can define an outer-most or overalldimension or length L1 that is measured along a line that extends alongor parallel to the curvature of the anatomical implant template 300 fromthe first terminal end surface 304 to the second terminal end surface306. For example, the length L1 can be measured parallel to a midlineML1 that extends from the first terminal end surface 304 to the secondterminal end surface 306 substantially midway between the first andsecond side surfaces 308 and 310. The midline ML1 can also extendsubstantially midway between the upper and lower surfaces 312 and 314 oralong one of the upper and lower surfaces 312 and 314. The length L1 isindependent of the curvature of the anatomical implant template 300, andtherefore, the length L1 remains constant as the curvature of theanatomical implant template 300 is changed. The anatomical implanttemplate 300 can also have a dimension D_(SL1) that is measured along astraight line SL1 from the first terminal end surface 304 to the secondterminal end surface 306. The dimension D_(SL1) is dependent on thecurvature of the anatomical implant template 300, and therefore, thedimension D_(SL1) can vary as the curvature of the anatomical implanttemplate 300 is changed.

The anatomical template implant 300 can further define an outer-most oroverall dimension or width W1 that is measured along a line that extendsalong or parallel to the curvature of the anatomical implant template300 from the first side surface 308 to the second side surface 310. Forexample, the width W1 can be measured parallel to a midline ML2 thatextends from the first side surface 308 to the second side surface 310substantially midway between the first and second terminal end surfaces304 and 306. The midline ML2 can also extend substantially midwaybetween the upper and lower surfaces 312 and 314 or along one of theupper and lower surfaces 312 and 314. The width W1 is independent of thecurvature of the anatomical implant template 300, and therefore, thewidth W1 remains constant as the curvature of the anatomical implanttemplate 300 is changed. The anatomical implant template 300 can alsohave a dimension D_(SL2) that is measured along a straight line SL2 fromthe first side surface 312 to the second side surface 314. The dimensionD_(SL2) is dependent on the curvature of the anatomical implant template300, and therefore, the dimension D_(SL2) can vary as the curvature ofthe anatomical implant template 300 is changed.

The anatomical template implant 300 can yet further define an outer-mostor overall thickness T1 that is measured from the upper surface 312 tothe lower surface 314. The thickness T1 is independent of the curvatureof the anatomical implant template 300, and therefore, the thickness T1remains constant as the curvature of the anatomical implant template 300is changed. The length L1 and width W1 can be greater than the thicknessT1, and in at least some embodiments, the length L1 can be greater thanthe width W1. The length L1, width W1, and thickness T1 of theanatomical implant template 300 can be any length L1, width W1, andthickness T1 suitable for attaching to the at least one anatomical body.For example, in embodiments wherein the anatomical implant template 300is used in a spine, the anatomical implant template 300 can have alength L1 that is sized to extend along at least two bodies such asalong at least two vertebrae or along at least one vertebra and theskull or sacrum.

The anatomical implant template 300 is configured to bend between thefirst terminal end surface 304 and the second terminal end surface 306and between the opposed first and second side surfaces 308 and 310. Theanatomical implant template 300 can be configured to bend at one or morebending locations along at least a portion of the anatomical implanttemplate 300 between the first and second terminal end surfaces 304 and306 and between the opposed first and second side surfaces 308 and 310.In at least some embodiments, the anatomical implant template 300 canbend continuously along at least a portion, up to an entirety, of theanatomical implant template 300 that extends between the first andsecond terminal end surfaces 304 and 306 and between the opposed firstand second side surfaces 308 and 310.

For example, the anatomical implant template 300 can include a bendinglocation that extends along at least a portion, up to an entirety, ofthe length L1 of the anatomical implant template 300 and along at leasta portion, up to an entirety, of the width W1 of the anatomical implanttemplate 300. Alternatively, the anatomical implant template 300 caninclude a plurality of bending locations, each of which extendscontinuously along a different portion of the anatomical implanttemplate 200 between the first terminal end surface 304 to the secondterminal end surface 306 and between the first side surface 308 to thesecond side surface 310. Alternatively still, the bending locations canbe defined by discrete bending points that are spaced from one anotherbetween the first and second terminal end surfaces 304 and 306 and/orbetween the opposed first and second side surfaces 308 and 310. Forexample, the anatomical implant template 300 can be configured to bendalong discrete points that are spaced from one another along (i) a linethat extends between the first and second terminal end surfaces 304 and306 and/or (ii) a line that extends between the opposed first and secondside surfaces 308 and 310. For illustrative purposes, FIG. 10 shows theanatomical implant template 300 having one bend; however, the user canbend the template body 202 so as to have more than one bend.

The anatomical implant template 300 is configured to bend at the bendinglocations so as to change the anatomical implant template 300 from afirst configuration to a second configuration. In at least someembodiments, the first configuration is an initial or pre-operativeconfiguration, and the second configuration is a subsequent orpost-operative configuration, where the subsequent or post-operativeconfiguration can conform more closely to the desired, post-operativecurvature or contour of the at least one anatomical body than theinitial or pre-operative configuration.

In the first configuration, the anatomical implant template 300 extendsfrom the first terminal end surface 304 to the second terminal endsurface 306 along a first path P1, and in the second configuration, theanatomical implant template 300 extends from the first terminal endsurface 304 to the second terminal end surface 306 along a second pathP2, different from the first path P1. The first and second paths P1 andP2 can be parallel to one or more of the midline ML1, the upper surface312, and the lower surface 314. The first path P1 has a first curvature,and the second path P2 has a second curvature, different from the firstcurvature.

Moreover, in the first configuration, the anatomical implant template300 extends from the first side surface 308 to the second side surface310 along a third path P3, and in the second configuration, theanatomical implant template 300 extends from the first side surface 308to the second side surface 310 along a fourth path P4, different fromthe third path P3. The third and fourth paths P3 and P4 can be parallelto one or more of the midline ML2, the upper surface 312, and the lowersurface 314. The third path P3 has a third curvature, and the fourthpath P4 has a fourth curvature, different from the third curvature.

It will be understood that the first to fourth paths P1 to P4 shown inFIGS. 9 and 10 are merely examples and that, in practice, the first tofourth paths P1 to P4, and hence the first to fourth curvatures, canvary from that shown in FIGS. 9 and 10. The first and third paths P1 andP3 may extend along straight lines as shown or can define any suitablecurvature. Further, the second and fourth paths P2 and P4 may extendalong parabolic curves as shown or can define any other suitablecurvature to match the curvature of the at least one anatomical body. Inat least some embodiments, the anatomical implant template 300 isfurther configured to be bent at one or more of the bending locations soas to change the template body from the second configuration back to thefirst configuration, or to a third configuration that is different fromboth the first and second configurations.

The anatomical implant template 300 can be configured to bend alongmultiple planes. In particular, the anatomical implant template 300 canbe configured to bend at each of the bending locations about an axis Aof rotation that extends through the anatomical implant template 300,where the axis A of rotation can extend through the anatomical implanttemplate 300 in any direction in a three dimensional space. For example,the axis A of rotation may extend through the anatomical implanttemplate 300 at the bending location between the first and secondterminal end surfaces 304 and 306 in a direction that is parallel to thefirst midline ML1. Thus, when the anatomical implant template 300 isbent about the axis A of rotation, the anatomical implant template 300curves from the first side surface 308 to the second side surface 310such that the first side surface 308 moves closer to the second sidesurface 310. As another example, the axis A of rotation may extendbetween the first and second side surfaces 308 and 310 in a directionthat is parallel to the second midline ML2. Thus, when the anatomicalimplant template 300 is bent about the axis of rotation, the anatomicalimplant template 300 curves from the first terminal end surface 304 tothe second terminal end surface 306, and the first terminal end surface304 moves closer to the second terminal end surface 306. Additionally oralternatively, the axis A of rotation may extend between any pair of thefirst terminal end surface 304, the second terminal end surface 306, thefirst side surface 308, and the second side surface 310 at any anglebetween the first and second midlines ML1 and ML2. For example, the axisA of rotation may extend through the anatomical implant template 300from the first terminal end surface 304 to the second side surface 310so as to bend the anatomical implant template 300 at that the upperright-hand corner of the anatomical implant template 300.

For illustrative purposes, FIG. 10 shows one point 316 that defines apeak of the curvature of the anatomical implant template 300, where thepeak 316 is at a geometric center of the anatomical implant template300. The anatomical implant template 300 has first and second axes A1and A2 of rotation that extend through the peak 316. The first axis A1of rotation is coincident with the second midline ML2 and the secondaxis A2 of rotation is coincident with the first midline ML1. As aresult, the anatomical implant template 300 is bent such that (i) theanatomical implant template 300 curves from the first side surface 308to the second side surface 310 so as to bring the first and second sidesurfaces 308 and 310 closer together, and (ii) anatomical implanttemplate 300 curves from the first terminal end surface 304 to thesecond terminal end surface 306 so as to bring the first and secondterminal end surfaces 304 and 306 closer together.

Note that the anatomical implant template 300 can additionally oralternatively define at least one peak that is not at the geometriccenter of the anatomical implant template 300 and can further definemore than one peak so as to have more than one curve. For example, theanatomical implant template 300 can have a peak that is located oneither side of the first midline ML1 and/or on either side of the secondmidline ML2. Thus, the anatomical implant template 300 can be bent aboutaxes of rotation that are not coincident with the first and/or thesecond midlines ML1 and/or ML2. In other words, the anatomical implanttemplate 300 can bend on either side of the first midline ML1 and/or oneither side of the second midline ML2. The anatomical implant template300 may have multiple such second axes of rotation between the first andsecond terminal end surfaces 304 and 306 and/or between the first andsecond side surfaces 308 and 310.

In the first configuration, the anatomical implant template 300 candefine a first radius R1 of curvature at the point 316, where the firstradius R1 of curvature lies in a first plane that is coincident with, orparallel to, the first axis A1 of rotation and/or perpendicular to thesecond axis A2 of rotation. Further, in the first configuration, theanatomical implant template 300 can also define a third radius R3 ofcurvature at the point 316, where the third radius R3 of curvature liesin a second plane that is coincident with, or parallel to, the secondaxis A2 of rotation and/or perpendicular to the first axis A1 ofrotation. In the second configuration, the anatomical implant template300 defines a second radius R2 of curvature at the point 316, where thesecond radius R2 of curvature lies in the first plane, and the secondradius R2 of curvature is different from the first radius R1 ofcurvature. In the second configuration, the anatomical implant template300 can also define a fourth radius R4 of curvature at the bendinglocation 316, where the fourth radius R4 of curvature lies in the secondplane, and the fourth radius R4 of curvature is different from the thirdradius R3 of curvature.

Turning now to FIGS. 11 to 13, various embodiments of the anatomicalimplant template 200 of FIGS. 9 and 10 are shown. In each embodiment,the anatomical implant template 300 includes a template body 302 and atleast one sensor 324 coupled to the template body 302. The template body302 is configured to bend so as to change the anatomical implanttemplate 300 from the first configuration to the second configuration.The at least one sensor 324 is configured to output at least one sensorsignal from which the curvature of the anatomical implant template 300in the second configuration can be ascertained.

The template body 302 includes a flexible body 318 that extends along,or substantially parallel to, (i) the midline ML1 between the first andsecond terminal end surfaces 304 and 306, and (ii) the midline ML2between the first and second side surfaces 308 and 310. The flexiblebody 318 can extend from the first terminal end surface 304 toward thesecond terminal end surface 306, and terminate at or before the secondterminal end surface 306. Similarly, the flexible body 318 can extendfrom the second terminal end surface 306 toward the first terminal endsurface 304, and terminate at or before the first terminal end surface304. Alternatively, the template body 302 can extend along a portion orportions of the anatomical implant template 300 between the first andsecond terminal end surfaces 304 and 306, and terminate before one orboth of the first and second terminal end surfaces 304 and 306.

In other words, the template body 302 can have a first terminal end anda second terminal end. The first terminal end of the template body 302can be coincident with the first terminal end surface 304 of the implanttemplate 300 or can be located between the first and second terminal endsurfaces 304 and 306. Similarly, the second terminal end of the templatebody 302 can be coincident with the second terminal end surface 304 orcan be located between the first and second terminal end surfaces 304and 306.

The flexible body 318 can extend from the first side surface 308 towardthe second side surface 310, and terminate at or before the second sidesurface 310. Similarly, the flexible body 318 can extend from the secondside surface 310 toward the first side surface 308, and terminate at orbefore the first side surface 308. Alternatively, the template body 302can extend along a portion or portions of the anatomical implanttemplate 300 between the first and second side surfaces 308 and 310, andterminate before one or both of the first and second side surfaces 308and 310.

In other words, the template body 302 can have a first side and a secondside. The side of the template body 302 can be coincident with the firstside surface 308 of the implant template 300 or can be located betweenthe first and second side surfaces 308 and 310. Similarly, the secondside of the template body 302 can be coincident with the second sidesurface 308 or can be located between the first and second side surfaces308 and 310.

The flexible body 318 can include any suitable malleable material orcombination of malleable materials that permits the template body 302 tobe conformed to the desired post-operative contour of the at least oneanatomical body. The malleable material or combination of materials mayinclude one or more of a metal such as annealed aluminum, a metal alloysuch as Nitinol, and a polymer. The flexible body 318 can include aplastically-deformable material configured to maintain the template body302 in the second configuration. Alternatively, or in addition, theflexible body 318 can include an elastically-deformable materialconfigured to return the template body 302 to the first configurationfrom the second configuration.

With continuing reference to FIGS. 9 to 13, the anatomical implanttemplate 300 supports at least one sensor 324 along or substantiallyparallel to (i) the midline ML1 between the first and second terminalend surfaces 304 and 306 and (ii) the midline ML2 between the first andsecond side surfaces 308 and 310. The at least one sensor 324 isconfigured output at least one sensor signal from which the shape of theanatomical implant template 300 in the second configuration can beascertained. The at least one sensor 324 can include a sensor body 326having a first terminal sensor end 326 a, a second terminal sensor end326 b spaced from the first terminal sensor end 326 a along the midlineML1, a first sensor side 326 c, a second sensor side 326 d spaced fromthe first sensor side 326 c along the midline ML2, an upper surface 326e, and a lower surface 326 f space from the upper surface along adirection that is perpendicular to both the first and second midlinesML1 and ML2. The lower surface 326 can be configured to face the atleast one anatomical body. In at least some embodiments, the sensor body326 can be elongate from the first terminal sensor end 326 a to thesecond terminal sensor end 326 b.

The sensor body 326 can extend from the first terminal end surface 304of the implant template 300 toward the second terminal end surface 306of the implant template 300, and terminate at or before the secondterminal end surface 306. Additionally or alternatively, the sensor body326 can extend from the second terminal end surface 306 toward the firstterminal end surface 304, and terminate at or before the first terminalend surface 304. The sensor body 326 can extend from the first sidesurface 308 toward the second side surface 310, and terminate at orbefore the second side surface 210. Additionally or alternatively, thesensor body 326 can extend from the second side surface 310 toward thefirst side surface 308, and terminate at or before the first sidesurface 310. Thus, the sensor body 326 can extend along a portion orportions of the template body 302 between the first and second terminalend surfaces 304 and 306 such that the sensor body 226 terminates at orbefore one or both of the first and second terminal end surfaces 304 and306 and between the first and second side surfaces 308 and 310 such thatthe sensor body 326 terminates at or before one or both of the first andsecond side surfaces 308 and 310.

The sensor body 326 can be coupled to the template body 302 such that atleast a portion of the sensor body 326 is aligned with at least one ofthe bending locations along a direction that is perpendicular to theupper and lower surfaces 312 and 314 of the implant template 300.Accordingly, when the template body 302 is bent at the at least onebending location, the sensor body 326 is also bent at the at least onebending location.

Alternatively or in addition, the at least one sensor 324 can include aplurality of discrete sensor bodies 326 spaced from one another betweenthe first and second terminal end surfaces 304 and 306 and between thefirst and second side surfaces 308 and 310. When discrete sensor bodies326 are employed, changes in the shape of the template body 302 betweenthe discrete sensors can be determined through extrapolation. In eithercase, the elongate sensor body 326 and/or the plurality of discretesensor bodies 326 can be coupled to the template body 302 so as to bealigned with at least one of the bending locations such that the atleast one sensor 324 bends at the at least one bending location.Alternatively, the sensor body 324 and/or the plurality of discretesensor bodies 324 can be coupled to the template body 302 so as to bepositioned between (i) at least one of the bending locations and (ii)another of the bending locations, the first terminal end surface 304,the second terminal end surface 306, the first side surface 308, or thesecond side surface 310 such that a position of the at least one sensor324 changes relative to the at least one of the bending locations as thetemplate body 302 is bent about the at least one of the bendinglocations.

The at least one sensor 324 can include any suitable sensor orcombination of sensors that can sense the shape of the template body 324in the second configuration. The at least one sensor 220 can be anactive sensor that actively transmits a signal or a passive sensor. Theat least one sensor 324 can include, for example, one or more positionsensors that measure absolute position of the template body 302 in thesecond configuration or relative position such as displacement of thetemplate body 302 from the first configuration to the secondconfiguration. In at least some embodiments, the at least one sensor 324can include one or more piezoelectric sensors as described above inrelation to the at least one sensor 220. The piezoelectric sensors canbe used to measure changes in or more of pressure, strain, and force,and convert these measured changes into at least one sensor signal. Inat least some embodiments, the at least one sensor 324 can include anoptical sensor as described above in relation to the at least one sensor220. The at least one sensor signal can be, for example, an electricalsignal or an optical signal.

Turning now to FIG. 11, an embodiment is shown in which the templatebody 302 includes a flexible body 318 and can optionally include aprotective covering 320. The flexible body 318 defines a plate thatextends between the first terminal end surface 304 and the secondterminal end surface 306 of the template body 302 and between the firstside surface 308 and the second side surface 310.

The protective covering 320 can cover at least a portion of the flexiblebody 318 between the first and second terminal end surfaces 304 and 306and between the first and second side surfaces 308 and 310. Further, theprotective covering can cover the first and second terminal end surfaces304 and 306 and the first and second side surfaces 308 and 310. Theprotective covering 320 has an inner surface that defines a channel 322that extends at least partially through the protective covering 320. Theflexible body 318 and the at least one sensor 324 are sized to bereceived in the channel 322 such that the at least one sensor 324 issupported between the flexible body 318 and at least a portion of theprotective covering 320. In alternative embodiments, the template body320 can define a channel that extends through the flexible body 318,such that the at least one sensor 324 is received in the channel andcoupled to the flexible body 318.

With continued reference to FIG. 11, the at least one sensor 324includes a flexible sensor body 326 that is planar so as to define athin plate or sheet that extends between the first and second terminalend surfaces 304 and 306 of the template body 302 and/or between thefirst and second side surfaces 308 and 310. Thus, the sensor body 326can extend along a portion or along a substantial entirety of thetemplate body 302. Further, the sensor body 326 can be coupled to thetemplate body 302 such that a portion of the sensor body 326 is alignedwith at least one, up to all, of the bending locations of the anatomicalimplant template 300. Accordingly, when the template body 302 is bent atthe at least one bending location, the sensor body 236 is also bent atthe at least one bending location. The at least one sensor 324 can beconfigured to sense bending at each location along a surface of thesensor body 326.

Alternatively or in addition, the at least one sensor 324 can include asensor grid, rather than a continuous elongate sensor, the sensor gridcovering at least a portion of the surface of the flexible body 318. Thesensor grid can include a plurality of sensor columns, each extendingbetween the first and second terminal end surfaces 304 and 306, and aplurality of sensor rows, each extending between the first and secondside surfaces 308 and 310. Each sensor row and/or each sensor column caninclude an elongate sensor or a plurality of discrete sensors spacedfrom one another. When discrete sensors are employed, changes in theshape of the elongate sensor body between the discrete sensors can bedetermined through extrapolation. In either case, the sensor body 326and the plurality of discrete sensors 326 can be coupled to the templatebody 302 so as to be aligned with at least one of the bending locationssuch that the at least one sensor 324 bends at the at least one bendinglocation. Alternatively, the sensor body 326 and/or the plurality ofdiscrete sensors 326 can be positioned between (i) at least one of thebending locations and (ii) another of the bending locations, the firstterminal end surface 304, the second terminal end surface 306, the firstside surface 308, or the second side surface 310 such that a position ofthe at least one sensor 324 changes relative to the at least one of thebending location as the template body 302 is bent about the at least oneof the bending locations.

Turning now to FIG. 12, an embodiment is shown in which the at least onesensor 324 is supported on the upper surface 312 of the anatomicalimplant template 300. In this embodiment, the at least one sensor 324 isplanar so as to define a thin strip or sheet that is mounted onto theupper surface 312. For instance, the at least one sensor 324 can be asticker that is adhered to the upper surface 312 or can be a strip thatis adhered to the surface via an adhesive. The at least one sensor 324can be removeably coupled to the flexible body 318 such that theflexible body 318 can be reused after cleaning as with conventionaltemplates. Further, the at least one sensor 324 can be disposable or canbe configured to survive cleaning such that the at least one sensor 324can be reused.

Referring to FIG. 13, an embodiment is shown in which the anatomicalimplant template 300 defines at least one channel 330 that extends intothe template body 302 toward the lower surface 314 such that the atleast one channel 330 is open opposite the lower surface 314. Toaccommodate each of the first and second channels 330 a and 330 b, thetemplate body 300 can optionally include at least one protrusion 332that extends above the upper surface 312 of the template body 302, wherethe at least one channel 330 extends into the at least one protrusion332.

The at least one channel 330 can define a first channel 330 a that iselongate between the first terminal end surface 304 and the secondterminal end surface 306. The at least one channel 330 can furtherdefine a second channel 330 b that is elongate between the first sidesurface 308 and the second side surface 310. The first and secondchannels 330 a and 330 b can overlap or intersect one another, and thefirst and second channels 330 a and 330 b can define any suitablecross-sectional shape, such as (without limitation) a circle as shown,an oval, a square, or a rectangle.

As shown in FIG. 14, the at least one sensor 324 can include a pair ofoverlapping elongate sensors 324 a and 324 b. The first sensor 324 a canbe elongate from a first terminal sensor end 326 a to a second terminalsensor end 326 b, and the second sensor 324 b can be elongate from thefirst sensor side 326 c to the second sensor side 326 c. The first andsecond sensors 324 a and 324 b can be press-fit into the first andsecond channels 330 a and 330 b, respectively. Alternatively, as shownin FIG. 15, the at least on sensor 324 can be a sheet sensor havingfirst and second sensors 324 a and 324 b.

Returning to FIGS. 9 and 10, the anatomical implant template 300 isconfigured to communicate the at least one sensor signal to a computingdevice such as computing device 104 of FIG. 1 via a wired or wirelessconnection. The at least one sensor can be configured to communicate theat least one sensor signal directly to the computing device.Alternatively, the anatomical implant template 300 can include at leastone transmitter 334 coupled to the template body 302 and configured tocommunicate the at least one sensor signal. The at least one transmitter334 can be supported anywhere by the template body 302, and can besupported such that the at least one transmitter 334 does not bend withthe template body 302. The at least one transmitter 334 can include awireless transmitter configured to wirelessly communicate the at leastone sensor signal to the computing device. Further, the at least onetransmitter 334 can include a power supply coupled to the template body302, where the power supply is configured to power the at least onetransmitter 334. Alternatively, the at least one transmitter 334 can bepowered by a power supply that is not coupled to the template body 302,such as a power supply that is coupled to a receiver such as an RFIDreceiver that senses the at least one sensor signal from a sensorcoupled to the template body 302. In the case of a wired connection, theanatomical implant template 300 can be coupled to a cable that carriesthe at least one sensor signal from the anatomical implant template 300to the computing device.

Referring to FIG. 16, a simplified flow diagram is shown of a method 400of operating the anatomical implant template 102 of FIG. 1 according toone embodiment. In step 402, the anatomical implant template 102 ispositioned along the at least one anatomical body. The positioningincludes bending the template body at one or more bending locations asdescribed above. For example, the positioning can include bending theanatomical implant template 102 between the first terminal end surfaceand the second terminal end surface of the template body so as to changethe template body from the first configuration to the secondconfiguration that conforms more closely to a contour or curvature ofthe at least one anatomical body than the first configuration. Theanatomical implant template 102 can be bent so as to avoid bending theanatomical implant template 102 at one or more securement locations thatare used to secure the anatomical-fixation implant to the at least oneanatomical body (e.g., at locations where the anatomical implanttemplate 102 is attached to a pedicle screw or adjacent to apertures inthe anatomical implant template 102 that receive bone screws).

Bending the anatomical implant template 102 at the one or more bendinglocations can include bending at least one sensor that is aligned withthe one or more bending locations. Alternatively, bending the anatomicalimplant template 102 at the one or more bending locations can includebending the anatomical implant template 102 such that at least onesensor spaced from the one or more bending locations is repositionedrelative to the one or more bending locations. The anatomical implanttemplate 102 can be plastically deformed such that the anatomicalimplant template 102 remains in the second configuration, or theanatomical implant template 102 can be elastically deformed such thatthe anatomical implant template 102 returns to the first configurationafter a bending force is removed.

Bending of the anatomical implant template 102 can be performed beforepositioning the anatomical implant template along the at least oneanatomical body, can be performed after positioning the anatomicalimplant template along the at least one anatomical body, or can beperformed concurrently with positioning the anatomical implant templatealong the at least one anatomical body. Step 402 can yet further includesecuring the anatomical implant template to the at least one anatomicalbody with at least one fixation device. The at least one fixation devicecan include, for example, at least one bone anchor such as a bone screwand/or hook. The at least one bone anchor can include a rod-receivingrecess to receive the anatomical implant template 102 in the case thatthe anatomical implant template 102 defines a rod shape. In embodimentsin which the anatomical implant template 102 defines a plate, the atleast one fixation device can include at least one screw or pin that isreceived through a hole defined in the anatomical implant template 102to secure the anatomical implant template 102 to bone underlying theanatomical implant template 102.

In step 404, the at least one sensor coupled to the anatomical implanttemplate 102 generates at least one signal 114 from which the shape ofthe anatomical implant template 102 in the second configuration can beascertained. For example, in embodiments where an optical sensor isused, the optical sensor can generate at least one sensor signal bymodifying an input light source. The at least one signal 114 can beindicative of the shape of the anatomical implant template 102 in thesecond configuration. For example, the at least one signal 114 can beindicative of absolute position of the anatomical implant template 102in the second configuration or relative position such as displacement ofthe anatomical implant template 102 from the first configuration to thesecond configuration.

Generating the at least one sensor signal can occur concurrently withbending of the anatomical implant template 102 or after bending of theanatomical implant template 102 has finished. The at least one sensorsignal can be generated in any manner described above or in any suitablealternative manner. In some embodiments, the anatomical implant template102 can include a processor coupled to the template body that processesthe at least one sensor signal. For example, the processor can performat least one of compression, amplification, filtering, and conversion ofthe signal from one format to another. The conversion can include, forexample, analog-to-digital conversion, optical-to-electronic conversion

In step 406, the anatomical implant template 102 communicates the atleast one sensor signal to the computing device 104. As described above,the communicating can include communicating the at least one sensorsignal via a wireless or wired connection. Further, the anatomicalimplant template 102 can communicate the at least one sensor signaldirectly from the at least one sensor to the computing device 104, suchthat the at least one sensor can be considered to be a transmitter, orcan communicate the at least one sensor signal to the computing device104 via a transmitter that is separate from the at least one sensor andthat is coupled to the anatomical implant template 102. The dataobtained from the at least one sensor signal can be used immediately inor near the operating room to fabricate the anatomical-fixation implant110 or can be used at a later time to fabricate the anatomical-fixationimplant 110 either in or near the operating room or at a location thatis remote from the operating room. Alternatively or additionally, thedata obtained from the at least one sensor signal can be aggregated forsubsequent and on-going analysis to improve patient outcomes.

Turning now to FIG. 17, a simplified flow diagram is shown of a method500 of manipulating the anatomical-fixation implant 110 of FIG. 1according to one embodiment. In step 502, the computing device 104receives data that can be used to determine a desired post-operativeshape for the anatomical-fixation implant 110. For example, the data caninclude the at least one signal 114 from the anatomical implant template102 as described above, where the at least one signal 114 carriesinformation from which the shape of the anatomical implant template 102in the second configuration can be ascertained. The at least one signal114 can be received via a wireless connection or via a wired connectionincluding one or more cables. Alternatively, the computing device 104can receive data obtained through another manner from which the desiredpost-operative shape of the anatomical implant template 102 can beascertained. For example, the data can be obtained using imagery orscans of an implant template at the surgical site. In such embodiments,the implant template can include at least one marker, such as at leastone reflective marker, that can be used to identify the shape of theanatomical implant template. Alternatively, the imagery can identify thelocations of screws or other fixation devices implanted at the surgicalsite, where the screws or other fixation devices will be used to attachthe anatomical-fixation implant 110 to the surgical site. In this case,the desired post-operative shape can be determined by modeling a line,such as a best fit line, through the screws or fixation devices.

In step 504, the computing device 104 generates implant bending signals116 that are used to bend the anatomical fixation implant 110. In atleast some embodiments, the computing device 104 can generate a3-dimensional computer model of the anatomical implant template oranatomical-fixation implant in the second configuration. Further, thecomputer model can be manipulated to allow for added correction notpresent in the anatomical-implant template, for example, when thesurgeon determines that added correction is appropriate for a specificpatient's conditions and/or indications. The implant bending signals 116can then be generated from the computer model or the manipulatedcomputer model.

In step 506, the computer-controlled bending machine 106 obtains implantbending signals that correspond to a shape of the anatomical-fixationimplant in a desired post-operative configuration, the shape having atleast one bent region. For example, the computing device 104 cancommunicate the implant bending signals 116 to the computer-controlledbending machine 106, which receives the anatomical-fixation implant 110in a first or pre-operative implant configuration 108. Theanatomical-fixation implant 110 in the pre-operative implantconfiguration 108 can be, for example, a rigid piece of stock materialthat is not bendable by hand. The computer-controlled bending machine106 may cut the anatomical-fixation implant 110 to a desired length, orthe anatomical-fixation implant 110 may be precut to the desired length.The computer-controlled bending machine 106, which can be situatedinside the operating room or at a location other than inside theoperating room, bends the anatomical-fixation implant 110 from the firstimplant configuration 108 to a second or post-operative implantconfiguration 112 using the implant bending signals 116 in step 506. Thepost-operative configuration 112 conforms to the curvature of theanatomical fixation template 102, and consequently to the curvature ofthe at least one anatomical body. The computer-controlled bendingmachine 106 bends the anatomical-fixation implant 110 such that theshape of the anatomical-fixation implant 110 changes in a manner similarto that described above in relation to the anatomical implant templatesof FIGS. 2 to 15. For example, the computer-controlled bending machine106 bends the anatomical-fixation implant 110 about one or more bendinglocations on the anatomical-fixation implant 110 and about one or moreaxes of rotation in a manner similar to that described above in relationto FIGS. 2 to 8 in the case of that the anatomical-fixation implant 110includes a rod and as described above in relation to FIGS. 9 to 15 inthe case that the anatomical-fixation implant 110 includes a plate.

In step 508, the anatomical implant template 102 is removed from the atleast one anatomical body, which can include bending the template bodyat the one or more bending locations so as to change the template bodyfrom the second configuration back to the first configuration. Note thatstep 508 can alternatively be performed prior to step 506 as long as theanatomical implant template 102 is maintained in the post-operativeconfiguration. In step 510, the anatomical-fixation implant 110 in thepost-operative configuration 112 is implanted by positioning theanatomical-fixation implant 110 along the at least one anatomical bodyand fixing the anatomical-fixation implant 110 to the at least oneanatomical body via one or more fixation devices. Theanatomical-fixation implant 110 may be positioned in a manner similar tothat described above in relation to the anatomical implant templates ofFIGS. 2 to 15. For example, the anatomical-fixation implant 110 can bepositioned in one or more of the sagittal plane and the coronal plane.As another example, the anatomical-fixation implant 110 can extendacross a plurality of anatomical bodies, such as at least two vertebraeor at least one vertebra and the skull or sacrum.

Fixing the anatomical-fixation implant 110 to the at least oneanatomical body can include manipulating the at least one anatomicalbody to achieve a desired curvature of the at least one anatomical body,and can be performed before or during the positioning theanatomical-fixation implant 110 along the at least one anatomical body.

It will be appreciated by those skilled in the art that changes could bemade to the embodiments described above without departing from the broadinventive concept thereof. Furthermore, it should be appreciated thatthe structure, features, and methods as described above with respect toany of the embodiments described herein can be incorporated into any ofthe other embodiments described herein unless otherwise indicated. It isunderstood, therefore, that this invention is not limited to theparticular embodiments disclosed, but it is intended to covermodifications within the spirit and scope of the present disclosure.Further, it should be appreciated, that the term substantially indicatesthat certain directional components are not absolutely perpendicular toeach other and that substantially perpendicular means that the directionhas a primary directional component that is perpendicular to anotherdirection.

What is claimed is:
 1. A method of determining a shape for an anatomicalimplant, the method comprising steps of: positioning an anatomicalimplant template along at least one anatomical body, the anatomicalimplant template defining first and second opposed terminal ends, andincluding a flexible body that extends between the first and secondopposed terminal ends, the flexible body having an external surface atleast partially covered by a protective covering, and an internalsurface opposite the external surface, the internal surface defining achannel therethrough that supports at least one sensor therein; bendingthe template from a first configuration, whereby the anatomical implanttemplate extends along a first path from the first terminal end to thesecond terminal end, to a second configuration, whereby the anatomicalimplant template extends from the first terminal end to the secondterminal end along a second path different from the first path, whereinwhen the anatomical implant template is in the second configuration, theanatomical implant template conforms more closely to a curvature of theat least one anatomical body as compared to when the template is in thefirst configuration; and causing the at least one sensor to generate asignal having information from which a shape of the anatomical implanttemplate in the second configuration can be ascertained; and causing atransmitter supported by the flexible body to wirelessly communicate thesignal to a computing device.
 2. The method of claim 1, comprisinggenerating, at the computing device, a computer model of the anatomicalimplant template in the second configuration from the at least onesensor signal.
 3. The method of claim 2, comprising bending ananatomical-fixation implant based on the computer model of theanatomical implant template so to conform the anatomical-fixationimplant to the curvature of the at least one anatomical body.
 4. Themethod of claim 3, comprising bending the anatomical-fixation implantwith a computer-controlled bending machine.
 5. The method of claim 1,wherein the positioning comprises implanting the anatomical implanttemplate onto the at least one anatomical body.
 6. The method of claim1, wherein the positioning comprises manipulating the at least oneanatomical body to achieve the curvature of the at least one anatomicalbody.
 7. The method of claim 1, wherein the positioning comprisesmanipulating the at least one anatomical body and the anatomical implanttemplate to achieve the curvature of the at least one anatomical body.8. The method of claim 1, wherein the transmitter is powered by a powersupply supported by the flexible body.
 9. The method of claim 1, whereinthe sensor is a piezoelectric sensor.
 10. The method of claim 1, whereinthe flexible body is made of metal.
 11. A method of manipulating ananatomical-fixation implant, the method comprising steps of: receivingat least one signal from a wireless transmitter of an anatomical implanttemplate having first and second opposed terminal ends, and a flexiblebody that extends between the first and second opposed terminal ends,the flexible body having an external surface at least partially coveredby a protective covering, and an internal surface opposite the externalsurface, the internal surface defining a channel therethrough thatsupports at least one sensor therein, the at least one signal includinginformation from which a shape of at least one bent region of theflexible body can be ascertained; generating implant bending signalsthat correspond to the at least one signal; and bending theanatomical-fixation implant based on the implant bending signals so asto include the at least one bent region.
 12. The method of claim 11,comprising bending the anatomical-fixation implant with acomputer-controlled bending machine.
 13. The method of claim 12, furthercomprising positioning the bent anatomical-fixation implant along the atleast one anatomical body.
 14. The method of claim 13, wherein thepositioning comprises securing the anatomical-fixation implant to the atleast one anatomical body with a fixation device.
 15. The method ofclaim 13, wherein the positioning comprises manipulating the at leastone anatomical body to achieve the curvature of the at least oneanatomical body.
 16. The method of claim 11, wherein theanatomical-fixation implant comprises a first terminal end, and a secondterminal end spaced from the first terminal end, and the bendingcomprises bending the anatomical-fixation implant from a firstconfiguration, wherein the anatomical-fixation implant extends from thefirst terminal end surface to the second terminal end surface along afirst path having a first curvature, to a second configuration, whereinthe anatomical-fixation implant extends from the first terminal endsurface to the second terminal end surface along a second path having asecond curvature, different from the first curvature.